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Boyd Research, Inc.

United StatesFDA 510(k) applicant, unverified FDA FEI 3010767848

Devices
2
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Boyd Research, Inc. makes

Boyd Research, Inc. manufactures oral appliance devices, including the ClenchGuard and NTI ClenchGuard, designed to manage temporomandibular joint disorders (TMD) and bruxism by repositioning the jaw and reducing clenching forces.

These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • ClenchGuard Ref K181005

    Unclassified
    Active 510(k) 510(k) —

  • NTI ClenchGuard Ref K211158

    Unclassified
    Active 510(k) 510(k) —

Company details

FDA FEI number
3010767848
Address
5820 Bali Way S, St Pete Beach, FL, 33706

Frequently asked questions

How many devices does Boyd Research, Inc. have in the registry?

The registry currently lists 2 devices for Boyd Research, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Boyd Research, Inc.'s devices?

Among its 2 most recently registered devices, Boyd Research, Inc. has devices listed in FDA 510(k) (2 devices).

What are the newest devices from Boyd Research, Inc. in the registry?

The most recently registered devices listed for Boyd Research, Inc. include ClenchGuard and NTI ClenchGuard.

Generated automatically from registry data and not verified by a human reviewer.